Genomic duplication ofPTPN11is an uncommon cause of Noonan syndrome
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference32 articles.
1. Noonan syndrome;Allanson;Am J Med Genet Part C,2007
2. Mouse model of Noonan syndrome reveals cell type- and gene dosage-dependent effects of Ptpn11 mutation;Araki;Nat Med,2004
3. Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication;Ballif;Mol Cytogenet,2008
4. Early fetal death associated with compound heterozygosity for Noonan syndrome-causative PTPN11 mutations;Becker;Am J Med Genet Part A,2007
5. Use of targeted array-based CGH for the clinical diagnosis of chromosomal imbalance: Is less more?;Bejjani;Am J Med Genet Part A,2005
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